http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102702145-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02E10-542
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01G9-20
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-30
filingDate 2012-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0b0a73682b6c4df2d24c4d9a90ecab6e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f52450c739a3a3184982ce2d7b383c9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a39cdf246f68ec73980a756a8dc07efc
publicationDate 2014-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102702145-B
titleOfInvention Triphenylamine derivative, preparation method and application thereof in dye sensitization solar cell
abstract The invention belongs to the technical field of dye sensitization solar cells and particularly relates to a triphenylamine derivative taking (E)-3-((E)-4-(di (4-((E)-4-(dianiline) styryl) phenyl)amino) as an electron donating group and cyanoacetic acid as an electron withdrawing group of furan, thiophene or styryl of benzene ring bridging. The invention also relates to a preparation method and the application of the triphenylamine derivative in a dye sensitization solar cell. The dye sensitization agent provided by the invention is simple in synthesis method, and tests show that the photoelectricity conversion efficiency of the final dye sensitization solar cell is up to 4.97 to 6.10 percent, therefore, the triphenylamine derivative and the preparation method is expected to be applied in the actual production to a certain degree.
priorityDate 2012-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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